US755808A - Sulfo-iodin compound of hydrocarbon. - Google Patents
Sulfo-iodin compound of hydrocarbon. Download PDFInfo
- Publication number
- US755808A US755808A US16259603A US1903162596A US755808A US 755808 A US755808 A US 755808A US 16259603 A US16259603 A US 16259603A US 1903162596 A US1903162596 A US 1903162596A US 755808 A US755808 A US 755808A
- Authority
- US
- United States
- Prior art keywords
- iodin
- compound
- sulfo
- hydrocarbon
- pounds
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 150000001875 compounds Chemical class 0.000 title description 13
- 239000004215 Carbon black (E152) Substances 0.000 title description 3
- 229930195733 hydrocarbon Natural products 0.000 title description 3
- 150000002430 hydrocarbons Chemical class 0.000 title description 3
- 239000000243 solution Substances 0.000 description 9
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical class C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 7
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical class [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 7
- 238000003756 stirring Methods 0.000 description 6
- 239000001257 hydrogen Substances 0.000 description 5
- 229910052739 hydrogen Inorganic materials 0.000 description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
- TUJKJAMUKRIRHC-UHFFFAOYSA-N hydroxyl Chemical compound [OH] TUJKJAMUKRIRHC-UHFFFAOYSA-N 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
- 239000001301 oxygen Substances 0.000 description 4
- 235000011121 sodium hydroxide Nutrition 0.000 description 4
- 229910052717 sulfur Inorganic materials 0.000 description 4
- 239000011593 sulfur Substances 0.000 description 4
- MGSRCZKZVOBKFT-UHFFFAOYSA-N thymol Chemical compound CC(C)C1=CC=C(C)C=C1O MGSRCZKZVOBKFT-UHFFFAOYSA-N 0.000 description 4
- 239000007789 gas Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- YQUVCSBJEUQKSH-UHFFFAOYSA-N 3,4-dihydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C(O)=C1 YQUVCSBJEUQKSH-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 241000282326 Felis catus Species 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 239000005844 Thymol Substances 0.000 description 2
- 235000011941 Tilia x europaea Nutrition 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- SURLGNKAQXKNSP-DBLYXWCISA-N chlorin Chemical compound C\1=C/2\N/C(=C\C3=N/C(=C\C=4NC(/C=C\5/C=CC/1=N/5)=CC=4)/C=C3)/CC\2 SURLGNKAQXKNSP-DBLYXWCISA-N 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- ORTFAQDWJHRMNX-UHFFFAOYSA-N hydroxidooxidocarbon(.) Chemical compound O[C]=O ORTFAQDWJHRMNX-UHFFFAOYSA-N 0.000 description 2
- 239000004571 lime Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000012907 medicinal substance Substances 0.000 description 2
- KJFMBFZCATUALV-UHFFFAOYSA-N phenolphthalein Chemical compound C1=CC(O)=CC=C1C1(C=2C=CC(O)=CC=2)C2=CC=CC=C2C(=O)O1 KJFMBFZCATUALV-UHFFFAOYSA-N 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 description 2
- 229960000790 thymol Drugs 0.000 description 2
- BRRSNXCXLSVPFC-UHFFFAOYSA-N 2,3,4-Trihydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C(O)=C1O BRRSNXCXLSVPFC-UHFFFAOYSA-N 0.000 description 1
- GLDQAMYCGOIJDV-UHFFFAOYSA-N 2,3-dihydroxybenzoic acid Chemical class OC(=O)C1=CC=CC(O)=C1O GLDQAMYCGOIJDV-UHFFFAOYSA-N 0.000 description 1
- FCUBUGPGVCEURB-UHFFFAOYSA-N 3-methyl-2-propylphenol Chemical compound CCCC1=C(C)C=CC=C1O FCUBUGPGVCEURB-UHFFFAOYSA-N 0.000 description 1
- PGSWEKYNAOWQDF-UHFFFAOYSA-N 3-methylcatechol Chemical compound CC1=CC=CC(O)=C1O PGSWEKYNAOWQDF-UHFFFAOYSA-N 0.000 description 1
- GZIRHHHTUNYVBQ-UHFFFAOYSA-N C1=C(C)C=CC(C(C)C)=C1O.CC=1C(=C(C=CC1)O)CCC Chemical compound C1=C(C)C=CC(C(C)C)=C1O.CC=1C(=C(C=CC1)O)CCC GZIRHHHTUNYVBQ-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 241000272161 Charadriiformes Species 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- MBMLMWLHJBBADN-UHFFFAOYSA-N Ferrous sulfide Chemical compound [Fe]=S MBMLMWLHJBBADN-UHFFFAOYSA-N 0.000 description 1
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- SHOKWSLXDAIZPP-UHFFFAOYSA-N [4-(4-iodooxy-2-methyl-5-propan-2-ylphenyl)-5-methyl-2-propan-2-ylphenyl] hypoiodite Chemical compound C1=C(OI)C(C(C)C)=CC(C=2C(=CC(OI)=C(C(C)C)C=2)C)=C1C SHOKWSLXDAIZPP-UHFFFAOYSA-N 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- 230000002421 anti-septic effect Effects 0.000 description 1
- 229940064004 antiseptic throat preparations Drugs 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- RLSSMJSEOOYNOY-UHFFFAOYSA-N m-cresol Chemical compound CC1=CC=CC(O)=C1 RLSSMJSEOOYNOY-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000007721 medicinal effect Effects 0.000 description 1
- -1 methyl-hydroxy benzin Chemical compound 0.000 description 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 description 1
- 239000004570 mortar (masonry) Substances 0.000 description 1
- 239000000346 nonvolatile oil Substances 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- OIPPWFOQEKKFEE-UHFFFAOYSA-N orcinol Chemical compound CC1=CC(O)=CC(O)=C1 OIPPWFOQEKKFEE-UHFFFAOYSA-N 0.000 description 1
- IWDCLRJOBJJRNH-UHFFFAOYSA-N p-cresol Chemical compound CC1=CC=C(O)C=C1 IWDCLRJOBJJRNH-UHFFFAOYSA-N 0.000 description 1
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 1
- 229960001755 resorcinol Drugs 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000012047 saturated solution Substances 0.000 description 1
- 229910001961 silver nitrate Inorganic materials 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- HYHCSLBZRBJJCH-UHFFFAOYSA-M sodium hydrosulfide Chemical compound [Na+].[SH-] HYHCSLBZRBJJCH-UHFFFAOYSA-M 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C381/00—Compounds containing carbon and sulfur and having functional groups not covered by groups C07C301/00 - C07C337/00
- C07C381/12—Sulfonium compounds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M135/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing sulfur, selenium or tellurium
- C10M135/02—Sulfurised compounds
- C10M135/04—Hydrocarbons
Definitions
- My invention relates to the production of a new medicinal substance from those derivatives of benzin which contain one or more hydroxyl radicals alone or in combination with other radicals, in replacement of an equal number of hydrogen radicals of the benzin.
- this class of derivatives belong such compounds as mono-hydroxy benzin, C6H5OH, (phenol,) methyl-hydroxy benzin, CeHi-CHaOH, (ortho, meta or paracresol,) ortho, meta, and para-dihydroxy benzin, O6H4(OH)2, (pyrocatechin, resorcin, and hydroquinone,) dihydroxy-toluene, CGH3-CH3(OH)2, (orcin,) trihydroxy benzin, G6H3(OH)3, (pyrogalloh) ortho, meta, and para-hydroXy-benzoic acids, OtH4.0H.COOH, (salicylic, oxy-benzoic, and para-oxy-benzoic acids,) di-hydroxy-benz
- My invention is carried out as follows to make ten pounds of the substance:
- Gr Place six pints of chlorinated soda solution in each of twelve two-gallon bottles. To each add twelve ounces of solution E by pouring in a fine stream, constantly stirring the soda solution. If the temperature rises above 40 centigrade, cool the bottle by placing in OH- corn ce l free iodin, and upon combustion sulfur-dioxid is formed.
- a new chemical compound formed from an hydroxyl containing derivative of a hydrocarbon, by substituting the hydrogen of such hydrocarbonderivative by iodin and the oxygen by sulfur, being a very light brown powder, practically odorless, very slightly soluble in concentrated alkalies, and absolute alcohol, insoluble in water, and soluble in ether, chloroform, collodion and fixed oils.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
UNITED STATES Patented March 29, 1904.
PATENT OFFICE.
SULFO-IODIN COMPOUND OF HYDROCARBQN.
SPECIFICATION forming part of Letters Patent No. 755,808, dated March 2?, 1904.
Application filed June 22, 1903.
To all whom it mag concern.-
Be it known that I, FRANK T. F. STEPHEN- SON, a citizen of the United States, residing in the city of Detroit, in the county of Wayne and State of Michigan,have invented a certain new and useful Sulfo-Iodin Compound of Hydrocarbon Derived from the Benzin Series, of which the following is a description, whereby others skilled in the art may make and use the same.
My invention relates to the production of a new medicinal substance from those derivatives of benzin which contain one or more hydroxyl radicals alone or in combination with other radicals, in replacement of an equal number of hydrogen radicals of the benzin. To this class of derivatives belong such compounds as mono-hydroxy benzin, C6H5OH, (phenol,) methyl-hydroxy benzin, CeHi-CHaOH, (ortho, meta or paracresol,) ortho, meta, and para-dihydroxy benzin, O6H4(OH)2, (pyrocatechin, resorcin, and hydroquinone,) dihydroxy-toluene, CGH3-CH3(OH)2, (orcin,) trihydroxy benzin, G6H3(OH)3, (pyrogalloh) ortho, meta, and para-hydroXy-benzoic acids, OtH4.0H.COOH, (salicylic, oxy-benzoic, and para-oxy-benzoic acids,) di-hydroxy-benzoic acids, Gel I3 (OH)2.COOH, (protocatechuic acid,) tri-hydroxy-benzoic acid,
CGHZ- (OH)3. COOH,
- enumerated, since this list indicates with sufficient accuracy the class of compounds to which I refer. My invention relates to these compounds, in that I take any one of them and by suitable chemical reactions replace the oxygen of the hydroxyl radical with sulfur and the hydrogen of the hydroxyl radical with iodin, thus forming a new radical, (S1,) in this way making new chemical compounds that have not heretofore been described and which have great medicinal value as antiseptics.
I know that there have already been made and that there are in use certain medicinal compounds derived from hydroxyl containing derivatives of benzin, in which the hydrogen of the hydroxyl radical has been replaced by iodin; but myinvention is an improvement Serial No. 162,596. (Specimens) upon these compounds, inasmuchas I replace the oxygen of the hydroxyl radical with sulfur, thus producing thenew radical, (S1,) which gives to the compounds containing it new and valuable medicinal properties which cannot be secured by the presence of'iodin alone.
Reference may be made to the patent to Joseph Massinger' and Georg Vortmann, No. 446,875, dated February 24, 1891, for a product that is called Aristol by the manufacturers, in which the hydrogen in the hydroxyl 'radicals of the propyl-meta-cresol (thymol) is replaced by iodin. In my invention I make an improved medicinal substance from propylmeta-cresol, for I replace one or both of. the atoms of oxygen in the hydroxyl radicals of two molecules of propyl-metei-cresol with sulfur, and in this way I make a new and improved compound for medicinal use.
My invention is carried out as follows to make ten pounds of the substance:
A. Dissolve thirty-five pounds sodium hydrate in sevenand one-half gallons of water and cool. Place in four Wolff bottles, putting more in the two bottles that are to go nearest to the gas-generator. Having fittedup a hy drogen-sulfid generator, connect with the Wolff bottles, and pass the gas through the hydrogen-sulfid solution until it is completely saturated with the gas, thus forming sodium hydrosulfid. The gas should flow slowly, and the saturation will not be complete until all the iron sulfid that forms a charge for a tengallon generator has been used up and the alcid also. Mix the contents of the Wolff bott es.
B. Dissolve seven pounds sodium hydrate in six quarts ofwater, add five and one-fourth pounds of thymol, heat and stir until complete'solution of thymol. Cool.
C. Mix A and B, stir well, and add enough saturated solution of sodium hydrate to keep solution clear, if needed.
D. Dissolve 4.35 pounds potassium iodid in 3. 5 pints of water, by stirring and warming, ordissolve 1.5 pounds sodium hydrate in 2.75 pigts of water, and in this dissolve 3.2 pounds 10 111.
F. Make up eighty gallons of a solution of chlorinated soda as follows: Mix eighty pounds chlorid of lime with forty gallons of water, breaking up the lumps and then allow to stand thirty minutes. Filter and make filtrate up to forty gallons by washing the contents of the filter. Dissolve one-hundred and twenty pounds carbonate of soda or its equivalent in soda-ash (M. 5 pounds) in forty gallons of water and filter, if necessary. The water should be heated to nearly boiling. Mix the soda solution with the one from the clorid of lime, stir well, and set aside for an hour. Decant as much as will come off clear and filter the rest. ash till filtrate measures eighty gallons.
Gr. Place six pints of chlorinated soda solution in each of twelve two-gallon bottles. To each add twelve ounces of solution E by pouring in a fine stream, constantly stirring the soda solution. If the temperature rises above 40 centigrade, cool the bottle by placing in OH- corn ce l free iodin, and upon combustion sulfur-dioxid is formed.
Having now explained my improvement, what I claim as my invention, and desire to secure by Letters Patent, is
1. A new chemical compound, formed from an hydroxyl containing derivative of a hydrocarbon, by substituting the hydrogen of such hydrocarbonderivative by iodin and the oxygen by sulfur, being a very light brown powder, practically odorless, very slightly soluble in concentrated alkalies, and absolute alcohol, insoluble in water, and soluble in ether, chloroform, collodion and fixed oils.
cool water. Too high temperature will spoil the product by setting free some of the iodin, thus making the product red and wasting iodin. As soon as the precipitation is complete, as is shown by no more forming on stirring and supernatant liquid becoming clear, test a little of the liquid with excess of chlorin solution. If no color or precipitate appears, throw the precipitate into a centrifuge or on a rapid filter to get rid ofthe chlorin as rapidly as possible. Wash until free from alkali, as shown by phenolphthalein, and from chlorids, as shown by silver nitrate. Dry away from light in a current of air at a temperature not above 40 Centigrade.
H. l/Vh en perfectly dry, the lump should be very light brown in color, almost white, free from red, and easily friable. Pulverize in a mortar. Pass through sieves until the powder will pass through fine bolting-silk.
The reactions are probably expressed as s1 cat on. gat
I eas est \(33H1 2. A chemical compound formed from the hydroxyl containing derivatives of benzin having probably the formula SI Gal on. Jat
I cat on. c itv QIQOH H2
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US16259603A US755808A (en) | 1903-06-22 | 1903-06-22 | Sulfo-iodin compound of hydrocarbon. |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US16259603A US755808A (en) | 1903-06-22 | 1903-06-22 | Sulfo-iodin compound of hydrocarbon. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US755808A true US755808A (en) | 1904-03-29 |
Family
ID=2824300
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US16259603A Expired - Lifetime US755808A (en) | 1903-06-22 | 1903-06-22 | Sulfo-iodin compound of hydrocarbon. |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US755808A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2878293A (en) * | 1953-09-03 | 1959-03-17 | Chilean Nitrate Sales Corp | Iodonium compounds |
-
1903
- 1903-06-22 US US16259603A patent/US755808A/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2878293A (en) * | 1953-09-03 | 1959-03-17 | Chilean Nitrate Sales Corp | Iodonium compounds |
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